NDC 31722-889 – Fingolimod

Fingolimod Hydrochloride .5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC31722-889

Product details

Brand name
Fingolimod
Generic name
Fingolimod
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA207933
Marketed since
September 27, 2019
Listing expires
December 31, 2026
Pharmacologic class
Sphingosine 1-phosphate Receptor Modulator

Active ingredients

Uses, dosage, side effects and warnings for Fingolimod →

Package NDC codes (1)

Package NDCDescriptionSince
31722-889-3030 CAPSULE in 1 BOTTLE (31722-889-30)Sep 27, 2019

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